GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6901 - 6925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0111070
  • congenital bile acid synthesis defect 3
  • Aliases:
    • CBAS3
    • oxysterol 7-alpha-hydroxylase deficiency
Homo sapiens (human)
DOID:0111071
  • congenital bile acid synthesis defect 1
  • Aliases:
    • CBAS1
Homo sapiens (human)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Mus musculus (house mouse)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Homo sapiens (human)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Rattus norvegicus (Norway rat)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Caenorhabditis elegans
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Danio rerio (zebrafish)
DOID:0111074
  • progressive familial heart block type IA
  • Aliases:
    • PFHB1A
Homo sapiens (human)
DOID:0111074
  • progressive familial heart block type IA
  • Aliases:
    • PFHB1A
Mus musculus (house mouse)
DOID:0111074
  • progressive familial heart block type IA
  • Aliases:
    • PFHB1A
Drosophila melanogaster (fruit fly)
DOID:0111074
  • progressive familial heart block type IA
  • Aliases:
    • PFHB1A
Rattus norvegicus (Norway rat)
DOID:0111076
  • progressive familial heart block type IB
  • Aliases:
    • PFHB1B
Homo sapiens (human)
DOID:0111076
  • progressive familial heart block type IB
  • Aliases:
    • PFHB1B
Mus musculus (house mouse)
DOID:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Homo sapiens (human)
DOID:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Drosophila melanogaster (fruit fly)
DOID:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Saccharomyces cerevisiae S288C
DOID:0111077
  • pyruvate kinase deficiency of red cells
  • Aliases:
    • PK deficiency
    • hemolytic anemia due to red cell pyruvate kinase deficiency
    • pyruvate kinase deficiency of erythrocyte
Rattus norvegicus (Norway rat)
DOID:0111078
  • tibial muscular dystrophy
  • Aliases:
    • Finnish tibial muscular dystrophy
    • TMD
    • Tardive tibial muscular dystrophy
    • Udd myopathy
    • Udd type distal myopathy
    • distal titinopathy
Homo sapiens (human)
DOID:0111078
  • tibial muscular dystrophy
  • Aliases:
    • Finnish tibial muscular dystrophy
    • TMD
    • Tardive tibial muscular dystrophy
    • Udd myopathy
    • Udd type distal myopathy
    • distal titinopathy
Mus musculus (house mouse)
DOID:0111079
  • birdshot chorioretinopathy
  • Aliases:
    • BSCR
    • birdshot chorioretinitis
    • birdshot retinochoroiditis
    • birdshot retinochoroidopathy
    • vitiliginous choroiditis
Homo sapiens (human)
DOID:0111079
  • birdshot chorioretinopathy
  • Aliases:
    • BSCR
    • birdshot chorioretinitis
    • birdshot retinochoroiditis
    • birdshot retinochoroidopathy
    • vitiliginous choroiditis
Rattus norvegicus (Norway rat)
DOID:0111079
  • birdshot chorioretinopathy
  • Aliases:
    • BSCR
    • birdshot chorioretinitis
    • birdshot retinochoroiditis
    • birdshot retinochoroidopathy
    • vitiliginous choroiditis
Mus musculus (house mouse)
DOID:0111083
  • Fanconi anemia complementation group D2
  • Aliases:
    • FA4
    • FAD2
    • FANCD2
    • Fanconi pancytopenia type 4
Homo sapiens (human)
DOID:0111086
  • Fanconi anemia complementation group G
  • Aliases:
    • FANCG
Homo sapiens (human)
DOID:0111089
  • Fanconi anemia complementation group D1
  • Aliases:
    • FAD1
    • FANCD1
Homo sapiens (human)

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Last updated: December 9, 2024